Canonical Allele Identifier: PA645423227
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 228273
ClinVar RCV Id: RCV000220187 RCV000763361 RCV000844674 RCV001312196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asn122Asp
CA10576999
NM_002755.4:c.364A>G